Labelling of GMO’s in the USA

  • Date: 17th May 2016 10:00 AM PST | 01:00 PM EST
  • Duration:75Min
  • Product Code:GRC-90023



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This event will offer an overview of the status of GMO’s/Genetically Engineered foods in the USA, how they are regulated by the FDA, FDA’s Biotechnology Policy and Consultation program, and GMO labeling regulations around the world. U.S. State, federal and consumer initiatives to require GMO food labeling in the USA will be discussed, including the soon to be enacted Vermont GMO Labeling law 120. Useful regulatory references will also be provided.

Please provide key Learning Objectives of your Topic –a. To learn about the regulatory status of GMOs in the USA; b. To review worldwide GMO Labeling rules; c. To cover FDA’s Biotechnology policy; d. to review FDA’s Biotechnology Consultation program; e. to understand Vermont’s labeling law and the status of other state GMO Labeling proposals. f. To understand what’s happened re: federal GMO labeling legislation. g. to understand industry reaction to the GMO labeling issue.

Please mention the Areas you will be touching during the Session: Safety of GMOs, Regulatory status of GMOs in the USA, Worldwide GMO labeling regulations, FDA’s Biotechnology Policy, FDA’s Biotechnology Consultation Program, U.S. state & Consumer Initiatives re: GMO Labeling, and Vermont’s new Labeling Law 120.

Areas Covered in the Session :

  • Safety of GMOs
  • Regulatory status of GMO’s in the USA
  • Worldwide GMO labeling regulations
  • FDA’ s Position on GMO’s
  • FDA Biotechnology Policy
  • FDA Biotechnology Consultation Program
  • State and Consumer initiatives re: GMO Labeling
  • Vermont Labeling law

Inspector profile :

Norma Skolnik has over 35 years of regulatory experience working with the pharmaceutical and dietary supplement industries. She served as Director of Regulatory Affairs for the Americas for Cadbury Adams. Prior to that she was Director of Regulatory Affairs for the Adams Division of Pfizer and Associate Director of Regulatory Affairs for the Warner-Lambert company. She also served as Director of Regulatory Affairs for Lederle Consumer Healthcare and as Associate Director of Marketed Product Support for Lederle Laboratories and Associate Director of Regulatory Affairs for Wyeth. She currently works as a regulatory consultant.

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